ABO exon and intron analysis in individuals with the A(weak)B phenotype reveals a novel O(1v)-A(2 )hybrid allele that causes four missense mutations in the A transferase

BACKGROUND: Since the cloning in 1990 of cDNA corresponding to mRNA transcribed at the blood-group ABO locus, polymorphisms due to ethnic and/or phenotypic variations have been reported. Some subgroups have been explained at the molecular level, but unresolved samples are frequently encountered in t...

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Detalles Bibliográficos
Autores principales: Hosseini-Maaf, Bahram, Hellberg, Åsa, Rodrigues, Maria J, Chester, M Alan, Olsson, Martin L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC305365/
https://www.ncbi.nlm.nih.gov/pubmed/14617382
http://dx.doi.org/10.1186/1471-2156-4-17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC305365/
https://www.ncbi.nlm.nih.gov/pubmed/14617382
http://dx.doi.org/10.1186/1471-2156-4-17

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